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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281730Generated: November 1, 2026

4-[(2-methyl-1,3-thiazol-4-yl)methoxy]benzoic Acid → N-{4-methyl-3-[4-(2-methylthiazol-4-ylmethoxy)benzamido]phenyl}dibenzofuran-4-carboxamide

https://huagongshe.com/reaction/1281730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(2-methyl-1,3-thiazol-4-yl)methoxy]benzoic AcidHCID 4962840—
ReactantHCID 22594118HCID 22594118—
SolventDichloromethaneHCID 6344—
ProductN-{4-methyl-3-[4-(2-methylthiazol-4-ylmethoxy)benzamido]phenyl}dibenzofuran-4-carboxamideHCID 1842211524.6%

Reaction Steps

4-(2-Methylthiazol-4-ylmethoxy)benzoic acid (0.095 g) was added to a stirred mixture of N-(3-amino-4-methylphenyl)dibenzofuran-4-carboxamide (0.12 g), diisopropyethyllamine (0.2 ml), 2-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate(V) (0.134 g) and methylene chloride (22 ml) and the mixture was stirred at ambient temperature for 16 hours. The mixture was evaporated and the residue was purified by column chromatography on an ion exchange column (isolute SCX column) using initially a 1:1 mixture of ethyl acetate and methanol and then a 99:1 mixture of methanol and a saturated aqueous ammonium hydroxide solution as eluent. The product so obtained was triturated under ethyl acetate. There was thus obtained the title compound (0.051 g); NMR Spectrum: (DMSOd6) 2.25 (s, 3H), 2.65 (s, 3H), 5.2 (s, 2H), 7.15 (d, 2H), 7.25 (d, 1H),7.4-7.65 (m, 5H), 7.8-7.9 (m, 3H), 7.98 (d, 2H), 8.2 (d, 1H), 8.35 (d, 1H), 9.8 (d, 1H), 10.4 (s, 1H); Mass Spectrum: M+H+ 548.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455520B1
Source datasetuspto-grants-2002_09
ORD IDord-38daf654bff441a3a828ad9c875b41fa
Source noteuspto-grants-2002_09